As new clinical studies are designed and managed, each study should begin in a well-organized, well-planned manner. This online course assists the clinical study site in preparation for a new clinical study. Topics include identifying the research team, roles and responsibilities of the study coordinator vs. investigators, preparing for a prestudy site visit, review of study protocol, preparing the IRB application, setting up study files and the regulatory binder, and site initiation.
Other Credits: BRN: 16 CE hours.
Note: Elective for Professional Certificate in Clinical Trials Design and Management.
Course Number: FPM-40179
Credit: 2.00 unit(s)
Related Certificate Programs: Clinical Trials Design and Management
+ Expand All